ClinVar Miner

List of variants in gene DIS3L2 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_152383.4(DIS3L2):c.1170C>T (p.Leu390=) rs17272089
NM_152383.4(DIS3L2):c.1448G>A (p.Arg483Gln) rs148474013
NM_152383.4(DIS3L2):c.1488T>C (p.His496=) rs72998118
NM_152383.4(DIS3L2):c.2187C>T (p.Pro729=) rs75782436
NM_152383.4(DIS3L2):c.2646A>G (p.Ser882=) rs3811578
NM_152383.4(DIS3L2):c.34C>T (p.Pro12Ser) rs723044
NM_152383.4(DIS3L2):c.426C>T (p.Pro142=) rs73001172

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